CSV Validation Specialist - GxP & Pharma Expert
Katalyst-Healthcares-
Requirements: Min 5 years of CSV experience. experience supporting validation of GxP GEN AI based solutions is a major plus experience supporting mergers/acquisitions/divestitures is a major plus Experience in the Pharmaceutical, biotechnology, or medical device industry Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs. Experience in QA Methodologies, designing, reviewing and approving Test Plans, System/UAT test scripts and Test procedures. Strong verbal and written communication skills. Ability to work as a team player, lead a team or accomplish tasks without supervision. Ability to work with remote teams and support several changes/projects simultaneously. Ability to provide Validation guidance, timely reviews, and escalations to TQ management. #J-18808-Ljbffr Katalyst-Healthcares-
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...Johnson is currently recruiting for QA Validation Specialist II LVV! .This position will be located in... ...Oversee Computerized System Validation (CSV) Must ensure that the selection, validation... ...computerized system used as part of the GxP regulated using the manufacturing area...SuggestedTemporary workLocal areaMonday to FridayShift workDay shift- Danta Technologies in New Jersey is seeking a Validation Lead to oversee validation activities for GxP GEN AI based solutions and LSMV Safety and Pharmacovigilance systems. The role supports hybrid/remote work from Raritan, NJ, with a pay rate of $45/hr on W2 and collaboration...SuggestedRemote work
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...innovative immunotherapies for patients living with multiple myeloma. COMPANY : Legend Biotech USA, Inc JOB TITLE : Validation Specialist JOB DUTIES : Execute site validation activities to the current regulatory and site requirements and address...SuggestedPermanent employmentFull timeTemporary workFor contractorsLocal areaWorldwideFlexible hours$55k - $70k
Baldwin & Obenauf, Inc. is seeking a proofreader in Somerville, NJ. The role demands 5+ years of experience, particularly in healthcare and pharmaceutical materials. As a key member of the team, you will ensure accuracy in editing across client communications, maintaining...Remote jobFull timeContract workFreelance- ...The Validation Engineer is responsible for executing, maintaining, and continuously improving site validation activities to ensure that equipment, utilities, facilities, processes, and systems remain in a qualified and validated state and comply with current Good Manufacturing...
$72.8k - $80.1k
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational...Worldwide- ...Piper Companies is currently looking for an experienced ( CQV) Validation Engineer in Raritan, NJ to work for an innovative and growing pharmaceutical organization. The primary responsibility of this role is to assist with the IQ/OQ/PQ of new instruments/equipment...
$87.1k - $94.6k
...done. We're obsessed with how it will be done.Key ResponsibilitiesCQV Execution & Safety- Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety- Deliver C&Q activities in alignment with project schedules- Track and report...For contractorsWorldwide- Bristol Myers Squibb is seeking a Senior Specialist, Operations Supply Planner for a 12-month assignment in New Jersey. The role partners with internal and external sites to develop and execute supply plans, balance service levels with efficiency, and manage MRP using...
- Tris Pharma, Inc. in Monmouth Junction, NJ is seeking a Metrologist II to support analytical laboratories by calibrating and maintaining instrumentation such as HPLC/UPLC, UV-Vis, FTIR, and more under cGMP guidelines. The role involves collaboration with laboratory management...
- ...maintain GMP documentation, and follow SOPs and safety procedures to ensure compliant production. Requirements include 1+ year in pharma manufacturing, High School/GED, and Lean Six Sigma is a plus. The role offers an hourly rate with incentive opportunities. #J-18808...Hourly pay
$65k - $104.65k
Johnson & Johnson Innovative Medicine in Raritan, NJ is seeking a QA Validation Specialist II LVV to provide quality oversight for daily production activities in a controlled cGMP environment. You will collaborate with Janssen Biotech and Legend Biotech teams to ensure...$91.7k - $135k
Work Schedule Standard (Mon-Fri) Environmental Conditions Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Job Description The Engineer III, Manufacturing Engineering...Temporary workWork at office- ...We provide commissioning, qualification, validation, startup, project management, and other consulting... ...Documentation & Compliance Author GxP computer validation documentation (e.g.,... ...System & Industry Expertise Support CSV activities across various platforms...Worldwide
$160k - $220k
JobRx, Inc. is seeking a Medical Science Liaison (MSL) to build relationships with healthcare professionals focused on Cushing's Syndrome and related diseases. The role requires an advanced scientific degree and at least two years of experience in medical affairs. The MSL...- Recordati Rare Diseases, Inc. North America is seeking a Medical Science Liaison to serve as a field-based scientific expert focusing on Cushing's Syndrome, Cushing's Disease and Acromegaly. This role requires building peer-to-peer relationships with leading clinicians...
- ...R3 Technology Inc. seeks Validation Engineer or it Hillsborough NJ office to gather requirements to develop product-level requirements and assist with high level systems view of product design. Conduct multi-disciplined product and process performance testing for both...Work at officeRelocation
- ADESA, a Carvana-owned company, seeks a Title Administrator to process automotive titles in a customer-facing setting at our Manville, NJ site. You will greet visitors, assist with front-counter title needs, and verify title documentation for accuracy. Role requires DMV...
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- H&R Block, Inc. is seeking a seasonal Experienced Tax Professional to assist clients with diverse tax situations, deliver personalized recommendations, and build lasting relationships. The role involves in-person work at a local tax office and participation in an industry...Seasonal workWork at officeLocal area
$7,200 per month
...Sr Mobile Expert At T-Mobile, we invest in YOU! Our Total Rewards Package ensures that employees get the same big love we give our customers. All team members receive a competitive base salary and compensation package - this is Total Rewards. Employees enjoy multiple...Hourly payFull timeTemporary workPart timeWork experience placementLocal areaFlexible hours$51.48 per hour
Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global pharmaceutical manufacturing client in Raritan, NJ. No Third-Party, No Corp to Corp, No Sponsorship Now, Future...Hourly payContract workTemporary workLocal area- Manufacturing Engineer • Floor Oriented • 5-7 years of manufacturing / process engineering experience • bility to read prints • Proven record of continuous improvement • Fiberglass experience is a plus • utomotive / Agricultural experience is preferred ...
- .... Working cross-functionally during the startup phase, the incumbent will drive equipment readiness, validation support, and serve as a technical subject matter expert (SME) for process equipment throughout the facility lifecycle. Key Responsibilities: # Lead...
- ...: Quality Pro Services LLC is looking for a skilled Plumbing Expert to join our growing, family owned plumbing business in Middlesex... ...workmanship Ability to handle the physical demands of plumbing work Valid driver's license and clean driving record What We Offer:...Local area
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...closure within or across disciplines. Responsibilities: Lead process engineering activities in product line, including Process Validation, Cleaning Validation, Equipment Qualification (IQ/OQ/PQ), investigations to address root cause. Support and monitor Production...Temporary workLocal area- Saint Peter's Healthcare System in New Jersey is seeking a Radiation Therapy Technologist Per Diem in the Radiation Oncology department. The role performs simulation and delivers high-energy ionizing radiation, providing patient care across the lifespan from neonates to...Daily paid
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...with a clear case for production About you ~4 years building new manufacturing technology in chemicals coatings adhesives inks pharma advanced materials or a similar field in industry ~ A track record of introducing new manufacturing methods that has impacted...Full timeWork at officeWorldwideFlexible hours
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